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An exact treatment would take into account the dependence of the diffusion coefficients as functions of the ion concentrations together with the cross correlations, which can be modelled by considering the Onsager coefficients Lij. This improved approach, would probably lead to similar result in our case, though. Indeed, most of the process is controlled by the mutual diffusion of the electrolyte solutions and this phenomenon appears to be relatively independent on the electrolyte concentration. Mutual diffusion coefficients of simple ion salts are relatively close to the Nernst- Hartley value up to molar concentrations because the effect of the activity coefficients is somewhat compensated by the change of the Onsager coefficients Lij's
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